Ethicon Endo-surgery - ALB
FDA adverse event reports naming Ethicon Endo-surgery - ALB as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ETHICON ENDO-SURGERY - ALB.
- Total reports
- 4,470
- Deaths
- 36
- Injuries
- 521
- Malfunctions
- 3,882
Reports per year
54298
89399
74400
1,66001
62902
203
Source: FDA adverse event reports by year received, 1998–2003. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Stapler, SurgicalGAG1,898
- Instrument, Ultrasonic SurgicalLFL1,718
- Applier, Surgical, ClipGDO273
- Unit, Electrosurgical, Endoscopic (With Or Without Accessories)KNS221
- Laparoscope, General & Plastic SurgeryGCJ188
- Product code KOGKOG152
- Powered Laser Surgical InstrumentGEX18
- Apparatus, Suturing, Stomach And IntestinalFHM1
- Staple, ImplantableGDW1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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